Suntech Medical, Inc.: Medical Device Recall in 2019 - (Recall #: Z-2277-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

SunTech Medical Disposable, Neonate #4, 1-Tube, Male Bayonet, Blood Pressure Cuffs, Box of 20

Product Classification:

Class II

Date Initiated: June 3, 2019

Date Posted: August 21, 2019

Recall Number: Z-2277-2019

Event ID: 83070

Reason for Recall:

Product is mislabeled. The label on the package is for a size #4 cuff, but the incorrect size #3 cuff was placed in the package.

Status: Terminated

Product Quantity: 80 total cuffs affected; 4 Boxes of 20 cuffs

Code Information:

Catalog # 98-0400-98 Lot Number: A4H201

Distribution Pattern:

Pakistan

Voluntary or Mandated:

Voluntary: Firm initiated